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    THIS WEBINAR WILL SHOW YOU HOW TO WRITE, ORGANIZE, 2013 - Key Factors to Write an Effective Standard Operating Procedure (SOP) and Work Instructions (WIs) - Webinar by GlobalCompliancePanel

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    Website http://bit.ly/167pOKC | Want to Edit it Edit Freely

    Category Webinar, Health, Medical, Pharma, Clinical

    Deadline: July 25, 2013 | Date: July 25, 2013

    Venue/Country: USA, U.S.A

    Updated: 2013-07-05 18:07:44 (GMT+9)

    Call For Papers - CFP

    Overview: This webinar will instruct the participant on how to write, organize, and maintain SOPs and train personnel in a way that will ensure compliance in a way that is concise, reproducible and easy to follow. It will begin with a strategic view of SOPs in a company and how SOPs can help streamline operations in addition to ensuring regulatory compliance.

    This will be followed by explanation on how to get from regulations to the SOP. Finally, Best Practices for creating, implementing and maintaining SOPs using a risk based approach and getting SOPs ready for inspection will be presented.

    Why you should attend: Standard Operating Procedures (SOPs) are required by law for companies that are regulated by the Code of Federal Regulations such as Title 21 and Title 493. Yet there is no guidance on how to write, organize and maintain SOPs. Consequently, SOPs are frequently written in a way that makes compliance difficult or downright impossible. Worse, this often leads to many regulatory errors that first come to light during an FDA audit. This webinar will show you how to write, organize, and maintain SOPs and train personnel in a way that will ensure compliance in a way that is concise, reproducible and easy to follow.

    Areas Covered In the Session:

    SOPs and their relation to the regulations

    SOPs as part of the company's regulatory infrastructure

    SOP on SOPs and how to ensure conciseness, consistency and ease of use

    Risk Based approach on SOP Best Practices for creation and maintenance

    Training on SOPs

    Tools for SOP tracking and when is validation required

    What the FDA looks for in SOPs during an inspection

    Who will benefit:

    Anyone that creates / maintains SOPs

    VP, Director, Manager of any dept that writes SOPs or performs training

    QA / QC

    Regulatory Affairs

    Angela Bazigos, is the CEO of Touchstone Technologies Silicon Valley, Inc. "Your Passport to Compliance". She has 30 years of experience in the Lifesciences industry spanning Project Management, Quality Assurance and Regulatory Affairs and has a patent aimed at speeding up Software Compliance.

    NetZealous LLC,

    DBA GlobalCompliancePanel

    161 Mission Falls Lane,

    Suite 216, Fremont, CA 94539, USA

    USA Phone:800-447-9407

    Fax: 302-288-6884

    webinarsatglobalcompliancepanel.com

    http://www.globalcompliancepanel.com

    Event Link - http://bit.ly/167pOKC


    Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
    Disclaimer: ourGlocal is an open academical resource system, which anyone can edit or update. Usually, journal information updated by us, journal managers or others. So the information is old or wrong now. Specially, impact factor is changing every year. Even it was correct when updated, it may have been changed now. So please go to Thomson Reuters to confirm latest value about Journal impact factor.